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AgeAnno: a knowledgebase of single-cell annotation of aging in human
Aging is a complex process that accompanied by molecular and cellular alterations. The identification of tissue-/cell type-specific biomarkers of aging and elucidation of the detailed biological mechanisms of aging-related genes at the single-cell level can help to understand the heterogeneous aging...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825500/ https://www.ncbi.nlm.nih.gov/pubmed/36200838 http://dx.doi.org/10.1093/nar/gkac847 |
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author | Huang, Kexin Gong, Hoaran Guan, Jingjing Zhang, Lingxiao Hu, Changbao Zhao, Weiling Huang, Liyu Zhang, Wei Kim, Pora Zhou, Xiaobo |
author_facet | Huang, Kexin Gong, Hoaran Guan, Jingjing Zhang, Lingxiao Hu, Changbao Zhao, Weiling Huang, Liyu Zhang, Wei Kim, Pora Zhou, Xiaobo |
author_sort | Huang, Kexin |
collection | PubMed |
description | Aging is a complex process that accompanied by molecular and cellular alterations. The identification of tissue-/cell type-specific biomarkers of aging and elucidation of the detailed biological mechanisms of aging-related genes at the single-cell level can help to understand the heterogeneous aging process and design targeted anti-aging therapeutics. Here, we built AgeAnno (https://relab.xidian.edu.cn/AgeAnno/#/), a knowledgebase of single cell annotation of aging in human, aiming to provide comprehensive characterizations for aging-related genes across diverse tissue-cell types in human by using single-cell RNA and ATAC sequencing data (scRNA and scATAC). The current version of AgeAnno houses 1 678 610 cells from 28 healthy tissue samples with ages ranging from 0 to 110 years. We collected 5580 aging-related genes from previous resources and performed dynamic functional annotations of the cellular context. For the scRNA data, we performed analyses include differential gene expression, gene variation coefficient, cell communication network, transcription factor (TF) regulatory network, and immune cell proportionc. AgeAnno also provides differential chromatin accessibility analysis, motif/TF enrichment and footprint analysis, and co-accessibility peak analysis for scATAC data. AgeAnno will be a unique resource to systematically characterize aging-related genes across diverse tissue-cell types in human, and it could facilitate antiaging and aging-related disease research. |
format | Online Article Text |
id | pubmed-9825500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98255002023-01-10 AgeAnno: a knowledgebase of single-cell annotation of aging in human Huang, Kexin Gong, Hoaran Guan, Jingjing Zhang, Lingxiao Hu, Changbao Zhao, Weiling Huang, Liyu Zhang, Wei Kim, Pora Zhou, Xiaobo Nucleic Acids Res Database Issue Aging is a complex process that accompanied by molecular and cellular alterations. The identification of tissue-/cell type-specific biomarkers of aging and elucidation of the detailed biological mechanisms of aging-related genes at the single-cell level can help to understand the heterogeneous aging process and design targeted anti-aging therapeutics. Here, we built AgeAnno (https://relab.xidian.edu.cn/AgeAnno/#/), a knowledgebase of single cell annotation of aging in human, aiming to provide comprehensive characterizations for aging-related genes across diverse tissue-cell types in human by using single-cell RNA and ATAC sequencing data (scRNA and scATAC). The current version of AgeAnno houses 1 678 610 cells from 28 healthy tissue samples with ages ranging from 0 to 110 years. We collected 5580 aging-related genes from previous resources and performed dynamic functional annotations of the cellular context. For the scRNA data, we performed analyses include differential gene expression, gene variation coefficient, cell communication network, transcription factor (TF) regulatory network, and immune cell proportionc. AgeAnno also provides differential chromatin accessibility analysis, motif/TF enrichment and footprint analysis, and co-accessibility peak analysis for scATAC data. AgeAnno will be a unique resource to systematically characterize aging-related genes across diverse tissue-cell types in human, and it could facilitate antiaging and aging-related disease research. Oxford University Press 2022-10-06 /pmc/articles/PMC9825500/ /pubmed/36200838 http://dx.doi.org/10.1093/nar/gkac847 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Huang, Kexin Gong, Hoaran Guan, Jingjing Zhang, Lingxiao Hu, Changbao Zhao, Weiling Huang, Liyu Zhang, Wei Kim, Pora Zhou, Xiaobo AgeAnno: a knowledgebase of single-cell annotation of aging in human |
title | AgeAnno: a knowledgebase of single-cell annotation of aging in human |
title_full | AgeAnno: a knowledgebase of single-cell annotation of aging in human |
title_fullStr | AgeAnno: a knowledgebase of single-cell annotation of aging in human |
title_full_unstemmed | AgeAnno: a knowledgebase of single-cell annotation of aging in human |
title_short | AgeAnno: a knowledgebase of single-cell annotation of aging in human |
title_sort | ageanno: a knowledgebase of single-cell annotation of aging in human |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825500/ https://www.ncbi.nlm.nih.gov/pubmed/36200838 http://dx.doi.org/10.1093/nar/gkac847 |
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